Stäfa, Switzerland | Hybrid
6‑month full-time internship
Are you studying Audiology, Life Sciences, Public Health, or a healthcare-related field and want to gain hands-on experience in the medical device industry?
As an Intern in Clinical Affairs, you’ll gain practical insight into clinical evaluations, and post-market clinical follow-up and clinical research activities. You’ll work closely with clinical experts in a global, highly regulated environment and contribute to real projects supporting product launches across all Sonova hearing aid brands.
Your Key Activities
1. Supporting literature searches and reviews
2. Supporting clinical evaluations and post-market clinical follow-up activities
3. Assisting with clinical studies (documentation, coordination, execution)
4. Working with clinical data and documentation in compliance with regulatory standards
5. Contributing to training activities and expert sessions
6. You’ll rotate across tasks to gain broad exposure to Clinical Affairs rather than working on just one topic.
Your Profile
7. Enrolled student or recent graduate (preferably Master’s level) in Audiology, Hearing Care, Life Sciences, Public Health, or similar
8. Basic knowledge of clinical studies, clinical data, or study design
9. Strong interest in Clinical or Regulatory Affairs
10. Fluent English and intermediate German
11. Self-organized, motivated, curious, and a team player
12. Interest in databases, statistics, or clinical research tools
Why Join Us?
As one of the world’s leading hearing care providers headquartered in Switzerland, we’re committed to building an inclusive culture. We want to create an environment where you can balance a successful career with your commitments and interests outside of work, through our flexible hybrid working model.
We offer a wide range of training opportunities for both your professional and personal development, and there are exceptional growth opportunities with individual development plans.
13. Hands-on experience in Clinical Affairs
14. Exposure to global clinical processes and regulatory environments
15. Collaboration with international stakeholders
16. Fast-paced environment with frequent new product launches
17. Opportunity to build a strong professional network in medical devices #LI-NB1